Dr. Reddy's recalls allergy/congestion tablets with failed dissolution specs. These tablets may not release medication properly. Consumers should contact Dr. Reddy's for details.
Failed dissolution specifications
Dr. Reddy's recalls 30-tablet allergy and congestion medication due to failed dissolution specifications. This means the tablets might not release medication as intended, potentially reducing effectiveness.
The tablets failed to dissolve properly as specified, which could mean they don't release medication correctly. This might reduce effectiveness but does not cause immediate harm.
People who bought the 30-tablet allergy and congestion medication from Walmart in the U.S. are affected. Those with allergies or congestion symptoms are most at risk.
Check for the product name: Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended Release Tablets USP. Look for the lot number AC2103329A on the packaging.
Look for the lot number AC2103329A on the packaging to confirm if it's recalled.
The recall is for failed dissolution specifications, which may reduce effectiveness but does not cause immediate harm.
Check for the lot number AC2103329A on the packaging of the 30-tablet allergy and congestion medication.
The recall does not specify a remedy, so contact Dr. Reddy's for details.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0275-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0275-2022 from Dr. Reddy's. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
